A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6377845



Internal ID9509838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:154406746..154407969hg38UCSC Ensembl
OuterchrX:154406709..154408019hg38UCSC Ensembl
InnerchrX:153635087..153636305hg19UCSC Ensembl
OuterchrX:153635050..153636355hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381311
hg191306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664900
Supporting Variants
SamplesNA18988
Known GenesDNASE1L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6377845
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer